دورية أكاديمية

Development of a platform process for the production and purification of single‐domain antibodies

التفاصيل البيبلوغرافية
العنوان: Development of a platform process for the production and purification of single‐domain antibodies
المؤلفون: Crowell, Laura E., Goodwine, Chaz, Holt, Carla S., Rocha, Lucia, Vega, Celina, Rodriguez, Sergio A., Dalvie, Neil C., Tracey, Mary K., Puntel, Mariana, Wigdorovitz, Andrés, Parreño, Viviana, Love, Kerry R., Cramer, Steven M., Love, J. Christopher
المساهمون: Defense Advanced Research Projects Agency, Bill and Melinda Gates Foundation
المصدر: Biotechnology and Bioengineering ; volume 118, issue 9, page 3348-3358 ; ISSN 0006-3592 1097-0290
بيانات النشر: Wiley
سنة النشر: 2021
المجموعة: Wiley Online Library (Open Access Articles via Crossref)
الوصف: Single‐domain antibodies (sdAbs) offer the affinity and therapeutic value of conventional antibodies, with increased stability and solubility. Unlike conventional antibodies, however, sdAbs do not benefit from a platform manufacturing process. While successful production of a variety of sdAbs has been shown in numerous hosts, purification methods are often molecule specific or require affinity tags, which generally cannot be used in clinical manufacturing due to regulatory concerns. Here, we have developed a broadly applicable production and purification process for sdAbs in Komagataella phaffii ( Pichia pastoris) and demonstrated the production of eight different sdAbs at a quality appropriate for nonclinical studies. We developed a two‐step, integrated purification process without the use of affinity resins and showed that modification of a single process parameter, pH of the bridging buffer, was required for the successful purification of a variety of sdAbs. Further, we determined that this parameter can be predicted based only on the biophysical characteristics of the target molecule. Using these methods, we produced nonclinical quality sdAbs as few as 5 weeks after identifying the product sequence. Nonclinical studies of three different sdAbs showed that molecules produced using our platform process conferred protection against viral shedding of rotavirus or H1N1 influenza and were equivalent to similar molecules produced in Escherichia coli and purified using affinity tags.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1002/bit.27724
الإتاحة: https://doi.org/10.1002/bit.27724Test
حقوق: http://creativecommons.org/licenses/by/4.0Test/ ; http://creativecommons.org/licenses/by/4.0Test/
رقم الانضمام: edsbas.A00A5766
قاعدة البيانات: BASE